These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

269 related articles for article (PubMed ID: 18258490)

  • 1. Sharing genetic test results in Lynch syndrome: communication with close and distant relatives.
    Stoffel EM; Ford B; Mercado RC; Punglia D; Kohlmann W; Conrad P; Blanco A; Shannon KM; Powell M; Gruber SB; Terdiman J; Chung DC; Syngal S
    Clin Gastroenterol Hepatol; 2008 Mar; 6(3):333-8. PubMed ID: 18258490
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Patterns of family communication and preferred resources for sharing information among families with a Lynch syndrome diagnosis.
    Petersen J; Koptiuch C; Wu YP; Mooney R; Elrick A; Szczotka K; Keener M; Pappas L; Kanth P; Soisson A; Kohlmann W; Kaphingst KA
    Patient Educ Couns; 2018 Nov; 101(11):2011-2017. PubMed ID: 30097381
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Uptake of genetic testing by relatives of lynch syndrome probands: a systematic review.
    Sharaf RN; Myer P; Stave CD; Diamond LC; Ladabaum U
    Clin Gastroenterol Hepatol; 2013 Sep; 11(9):1093-100. PubMed ID: 23669308
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Improving the uptake of predictive testing and colorectal screening in Lynch syndrome: a regional primary care survey.
    Barrow P; Green K; Clancy T; Lalloo F; Hill J; Evans DG
    Clin Genet; 2015 Jun; 87(6):517-24. PubMed ID: 25652327
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Evaluating the utilization of educational materials in communicating about Lynch syndrome to at-risk relatives.
    Dilzell K; Kingham K; Ormond K; Ladabaum U
    Fam Cancer; 2014 Sep; 13(3):381-9. PubMed ID: 24770865
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sharing genetic risk with next generation: mutation-positive parents' communication with their offspring in Lynch Syndrome.
    Aktan-Collan KI; Kääriäinen HA; Kolttola EM; Pylvänäinen K; Järvinen HJ; Haukkala AH; Mecklin JP
    Fam Cancer; 2011 Mar; 10(1):43-50. PubMed ID: 20857224
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Extent of Pedigree Required to Screen for and Diagnose Hereditary Nonpolyposis Colorectal Cancer: Comparison of Simplified and Extended Pedigrees.
    Heo Y; Kim MH; Kim DW; Lee SA; Bang S; Kim MJ; Oh HK; Kang SB; Kang SI; Park JW; Ryoo SB; Jeong SY; Park KJ
    Dis Colon Rectum; 2020 Feb; 63(2):152-159. PubMed ID: 31842160
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic testing in families with hereditary colorectal cancer in British Columbia and Yukon: a retrospective cross-sectional analysis.
    Beard VK; Bedard AC; Nuk J; Lee PWC; Hong Q; Bedard JEJ; Sun S; Schrader KA
    CMAJ Open; 2020; 8(4):E637-E642. PubMed ID: 33077534
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Stakeholder Perspectives on Overcoming Barriers to Cascade Testing in Lynch Syndrome: A Qualitative Study.
    Srinivasan S; Hampel H; Leeman J; Patel A; Kulchak Rahm A; Reuland DS; Roberts MC
    Cancer Prev Res (Phila); 2020 Dec; 13(12):1037-1046. PubMed ID: 32727822
    [TBL] [Abstract][Full Text] [Related]  

  • 10. How families communicate about HNPCC genetic testing: findings from a qualitative study.
    Peterson SK; Watts BG; Koehly LM; Vernon SW; Baile WF; Kohlmann WK; Gritz ER
    Am J Med Genet C Semin Med Genet; 2003 May; 119C(1):78-86. PubMed ID: 12704641
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
    Yurgelun MB; Allen B; Kaldate RR; Bowles KR; Judkins T; Kaushik P; Roa BB; Wenstrup RJ; Hartman AR; Syngal S
    Gastroenterology; 2015 Sep; 149(3):604-13.e20. PubMed ID: 25980754
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Changes in screening behaviors and attitudes toward screening from pre-test genetic counseling to post-disclosure in Lynch syndrome families.
    Burton-Chase AM; Hovick SR; Peterson SK; Marani SK; Vernon SW; Amos CI; Frazier ML; Lynch PM; Gritz ER
    Clin Genet; 2013 Mar; 83(3):215-20. PubMed ID: 23414081
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic testing for Lynch syndrome: family communication and motivation.
    Leenen CH; Heijer Md; van der Meer C; Kuipers EJ; van Leerdam ME; Wagner A
    Fam Cancer; 2016 Jan; 15(1):63-73. PubMed ID: 26446592
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hereditary nonpolyposis colorectal cancer: diagnostic strategies and their implications.
    Bonis PA; Trikalinos TA; Chung M; Chew P; Ip S; DeVine DA; Lau J
    Evid Rep Technol Assess (Full Rep); 2007 May; (150):1-180. PubMed ID: 17764220
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice.
    Menko FH; Ter Stege JA; van der Kolk LE; Jeanson KN; Schats W; Moha DA; Bleiker EMA
    Fam Cancer; 2019 Jan; 18(1):127-135. PubMed ID: 29846880
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ten years after mutation testing for Lynch syndrome: cancer incidence and outcome in mutation-positive and mutation-negative family members.
    Järvinen HJ; Renkonen-Sinisalo L; Aktán-Collán K; Peltomäki P; Aaltonen LA; Mecklin JP
    J Clin Oncol; 2009 Oct; 27(28):4793-7. PubMed ID: 19720893
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relatives.
    Hunter JE; Arnold KA; Cook JE; Zepp J; Gilmore MJ; Rope AF; Davis JV; Bergen KM; Esterberg E; Muessig KR; Peterson SK; Syngal S; Acheson L; Wiesner G; Reiss J; Goddard KAB
    Fam Cancer; 2017 Jul; 16(3):377-387. PubMed ID: 28176204
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Communication of genetic test results to family and health-care providers following disclosure of research results.
    Graves KD; Sinicrope PS; Esplen MJ; Peterson SK; Patten CA; Lowery J; Sinicrope FA; Nigon SK; Borgen J; Gorin SS; Keogh LA; Lindor NM;
    Genet Med; 2014 Apr; 16(4):294-301. PubMed ID: 24091800
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Factors affecting encouragement of relatives among families with Lynch syndrome to seek medical assessment.
    Ishii N; Arai M; Koyama Y; Ueno M; Yamaguchi T; Kazuma K; Muto T
    Fam Cancer; 2011 Dec; 10(4):649-54. PubMed ID: 21695501
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Family communication about positive BRCA1 and BRCA2 genetic test results.
    McGivern B; Everett J; Yager GG; Baumiller RC; Hafertepen A; Saal HM
    Genet Med; 2004; 6(6):503-9. PubMed ID: 15545746
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.